Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700102P08Rik |
T |
A |
9: 108,270,439 (GRCm39) |
M1K |
probably null |
Het |
2810021J22Rik |
T |
C |
11: 58,771,166 (GRCm39) |
L216S |
possibly damaging |
Het |
4933405O20Rik |
G |
A |
7: 50,249,220 (GRCm39) |
E85K |
possibly damaging |
Het |
Agrn |
A |
G |
4: 156,257,492 (GRCm39) |
F1153L |
probably damaging |
Het |
Cbx8 |
A |
G |
11: 118,929,742 (GRCm39) |
S284P |
probably damaging |
Het |
Cep128 |
A |
G |
12: 91,305,893 (GRCm39) |
L170P |
probably damaging |
Het |
Cyp4f14 |
T |
A |
17: 33,126,959 (GRCm39) |
T324S |
probably damaging |
Het |
Daw1 |
G |
T |
1: 83,170,419 (GRCm39) |
V244L |
probably benign |
Het |
Eef2kmt |
A |
G |
16: 5,063,222 (GRCm39) |
V306A |
probably benign |
Het |
Enah |
A |
T |
1: 181,763,293 (GRCm39) |
|
probably null |
Het |
Fam171b |
T |
C |
2: 83,683,949 (GRCm39) |
|
probably null |
Het |
Fsip2 |
C |
T |
2: 82,808,925 (GRCm39) |
T1748I |
possibly damaging |
Het |
Gabrg2 |
C |
T |
11: 41,862,559 (GRCm39) |
G175D |
probably damaging |
Het |
Gtf2h3 |
C |
T |
5: 124,722,360 (GRCm39) |
T121I |
probably benign |
Het |
Hmcn1 |
G |
T |
1: 150,458,047 (GRCm39) |
N33K |
probably damaging |
Het |
Incenp |
T |
A |
19: 9,855,770 (GRCm39) |
E514V |
unknown |
Het |
Kank3 |
T |
C |
17: 34,036,917 (GRCm39) |
S74P |
probably benign |
Het |
Lrriq1 |
G |
T |
10: 103,051,206 (GRCm39) |
N515K |
probably benign |
Het |
Mfsd13b |
G |
A |
7: 120,591,056 (GRCm39) |
D266N |
probably damaging |
Het |
Neto1 |
T |
C |
18: 86,422,998 (GRCm39) |
Y152H |
probably damaging |
Het |
Nub1 |
C |
A |
5: 24,900,533 (GRCm39) |
F145L |
probably benign |
Het |
Nufip1 |
T |
C |
14: 76,351,715 (GRCm39) |
|
probably null |
Het |
Polr3a |
T |
C |
14: 24,505,009 (GRCm39) |
I1084V |
possibly damaging |
Het |
Rapgef5 |
A |
C |
12: 117,703,379 (GRCm39) |
N431T |
probably damaging |
Het |
Rassf9 |
A |
T |
10: 102,381,205 (GRCm39) |
T196S |
probably damaging |
Het |
Rrp12 |
T |
C |
19: 41,865,029 (GRCm39) |
Y764C |
probably benign |
Het |
Slfn8 |
T |
C |
11: 82,908,550 (GRCm39) |
|
probably null |
Het |
Smox |
T |
A |
2: 131,363,026 (GRCm39) |
V265D |
probably damaging |
Het |
Sult1b1 |
T |
C |
5: 87,678,510 (GRCm39) |
I105V |
probably benign |
Het |
Sycp2 |
T |
C |
2: 178,045,554 (GRCm39) |
D22G |
probably damaging |
Het |
Tbck |
G |
A |
3: 132,456,977 (GRCm39) |
M630I |
possibly damaging |
Het |
Tenm4 |
G |
C |
7: 96,486,538 (GRCm39) |
G965R |
possibly damaging |
Het |
Trappc10 |
G |
A |
10: 78,023,694 (GRCm39) |
T1258I |
probably damaging |
Het |
Tssk1 |
G |
A |
16: 17,713,123 (GRCm39) |
G303S |
probably benign |
Het |
Tstd2 |
T |
C |
4: 46,120,461 (GRCm39) |
Y313C |
probably damaging |
Het |
Usp42 |
G |
A |
5: 143,707,401 (GRCm39) |
T260M |
probably damaging |
Het |
Wdr43 |
T |
A |
17: 71,955,772 (GRCm39) |
V479E |
probably damaging |
Het |
Xpo7 |
G |
A |
14: 70,921,171 (GRCm39) |
T599I |
probably damaging |
Het |
Zfp553 |
A |
G |
7: 126,836,013 (GRCm39) |
K523E |
probably benign |
Het |
|
Other mutations in Pard6g |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01024:Pard6g
|
APN |
18 |
80,123,037 (GRCm39) |
splice site |
probably benign |
|
IGL01514:Pard6g
|
APN |
18 |
80,160,661 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01519:Pard6g
|
APN |
18 |
80,123,071 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02305:Pard6g
|
APN |
18 |
80,160,985 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03115:Pard6g
|
APN |
18 |
80,123,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R0411:Pard6g
|
UTSW |
18 |
80,160,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R0604:Pard6g
|
UTSW |
18 |
80,160,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R0938:Pard6g
|
UTSW |
18 |
80,123,259 (GRCm39) |
nonsense |
probably null |
|
R1730:Pard6g
|
UTSW |
18 |
80,123,040 (GRCm39) |
missense |
probably damaging |
0.97 |
R1783:Pard6g
|
UTSW |
18 |
80,123,040 (GRCm39) |
missense |
probably damaging |
0.97 |
R1785:Pard6g
|
UTSW |
18 |
80,160,523 (GRCm39) |
missense |
probably damaging |
0.96 |
R1786:Pard6g
|
UTSW |
18 |
80,160,523 (GRCm39) |
missense |
probably damaging |
0.96 |
R1851:Pard6g
|
UTSW |
18 |
80,160,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R2070:Pard6g
|
UTSW |
18 |
80,160,940 (GRCm39) |
missense |
probably benign |
0.00 |
R2132:Pard6g
|
UTSW |
18 |
80,160,523 (GRCm39) |
missense |
probably damaging |
0.96 |
R2133:Pard6g
|
UTSW |
18 |
80,160,523 (GRCm39) |
missense |
probably damaging |
0.96 |
R3778:Pard6g
|
UTSW |
18 |
80,123,038 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6084:Pard6g
|
UTSW |
18 |
80,160,420 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6913:Pard6g
|
UTSW |
18 |
80,160,534 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7124:Pard6g
|
UTSW |
18 |
80,160,340 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8109:Pard6g
|
UTSW |
18 |
80,160,658 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8469:Pard6g
|
UTSW |
18 |
80,090,347 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8903:Pard6g
|
UTSW |
18 |
80,160,411 (GRCm39) |
nonsense |
probably null |
|
R8915:Pard6g
|
UTSW |
18 |
80,160,957 (GRCm39) |
missense |
probably damaging |
0.99 |
R9077:Pard6g
|
UTSW |
18 |
80,160,772 (GRCm39) |
missense |
probably damaging |
0.99 |
|